morphine sulfate 1 mg per mL in 0 — Class II drug recall D-0064-2018
Terminated recall by SCA Pharmaceuticals, LLC, reported 2017-11-08, distributed nationwide. Lack Of Assurance Of Sterility.
| Recall number | D-0064-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SCA Pharmaceuticals, LLC, Little Rock, AR, United States |
| Recall initiated | 2017-10-19 |
| Classified | 2017-11-02 |
| Reported by FDA | 2017-11-08 |
| Terminated | 2019-05-01 |
| Distributed | Nationwide (US) |
| Reason classes | sterility |
| NDC | 70004-0100-22, 70004-0100-63 |
| Expiration dates | 2017-11-30, 2017-12-04 |
Product
morphine sulfate 1 mg per mL in 0.9% Sodium Chloride a) Total Volume 100 mL in Single Dose CADD Cassette (Total morphine Dose 100 mg per 100 mL) (NDC 70004-0100-63) b) Total Volume 50 mL in Single Dose Syringe (Total morphine Dose 50 mg / 50 mL) (NDC 70004-0100-22) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205
Reason for recall
Lack Of Assurance Of Sterility.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0064-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.